About   Help   FAQ
Disease Ontology Browser
benign familial infantile seizures 6 (DOID:0081119)
Alliance: disease page
Synonyms: Autosomal dominant nocturnal frontal lobe epilepsy; Benign Familial Infantile Seizures, 6; nocturnal frontal lobe epilepsy-4
Alt IDs: OMIM:610353
Definition: A benign familial infantile epilepsy that is characterized by afebrile partial complex or generalized tonic-clonic seizures occurring between 3 and 12 months of age with a good response to medication and no neurologic sequelae and that has_material_basis_in mutation in the CHRNA2 gene on chromosome 8p21.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory